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Congenital diaphragmatic hernia

4 OMIM references -
3 associated genes
1 sign/symptom

PROTEIN INTERACTIONS: 1

Benign familial chorea

2 OMIM references -
1 associated gene
2 signs/symptoms

Congenital diaphragmatic hernia

Benign familial chorea

FREM1	(UniProt - OMIM)		NKX2-1	(UniProt - OMIM)
GATA6	(UniProt - OMIM)
ZFPM2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GATA6	(0.72)	NKX2-1

Citations in the biomedical literature:

Congenital diaphragmatic hernia		Benign familial chorea
	Synonym(s): - CDH - Diaphragmatic agenesia		Synonym(s): - Hereditary benign chorea

	Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare respiratory disease - Rare surgical thoracic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: multigenic/multifactorial		Epidemiological data: (no data available)

	External references: 4 OMIM references - 1 MeSH reference: C538080		External references: 2 OMIM references - No MeSH references

Congenital diaphragmatic hernia		Benign familial chorea
	Very frequent - Diaphragmatic hernia / defect / agenesis		Very frequent - Abnormal gait - Movement disorder